FDA 510(k)

ACCUTEX CRP LATEX TEST

K-Number: K924332 · 1992-12-07

Decision Date1992-12-07

Product CodeDCK

Advisory CommitteeIM

DecisionSubstantially Equivalent

Device Summary

ACCUTEX CRP LATEX TEST is the device name listed in this FDA 510(k) record. The listed applicant is J.S. Medical Assoc.. It received FDA 510(k) clearance on 1992-12-07 under 510(k) number K924332. The device is classified under product code DCK. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCUTEX CRP LATEX TEST?

ACCUTEX CRP LATEX TEST is a medical device that received FDA 510(k) clearance on 1992-12-07. The listed applicant is J.S. Medical Assoc.. The 510(k) number is K924332.

When did ACCUTEX CRP LATEX TEST receive FDA 510(k) clearance?

ACCUTEX CRP LATEX TEST received FDA 510(k) clearance on 1992-12-07, under 510(k) number K924332.

Who is the listed applicant for ACCUTEX CRP LATEX TEST?

The FDA 510(k) record lists J.S. Medical Assoc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACCUTEX CRP LATEX TEST?

The FDA product code for ACCUTEX CRP LATEX TEST is DCK.

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Other records listing J.S. Medical Assoc. as applicant

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Related Devices (Code: DCK)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.